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I had never heard of a "Child Life Specialist" They're all over the hospital, and you can request to meet with them. Their job is to ensure the best possible hospital experience for patients, siblings and parents. Because they're not involved in the actual nursing care, they had time to spend with us. We met two of them yesterday.
Haley sat us down and went through a picture book with Tess about what her day of pre-op would be like. She had the O2 sensors, masks and caps, and other instruments that would be used to assess her later in the morning which allowed Tess to play with them, familiarize herself with them. When the time came to put the oxygen sensor on her finger, Tessa took it out of the nurse's hand and said, "I know how to do this one," and put it on her own finger all by herself.
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Haley called up to the child life specialist on the ICU and arranged for a tour for us. That was so helpful, as Tess will be staying in the ICU for observation on Monday night before being moved to a regular floor for the remainder of her time at the hospital. Again, the CLS was so friendly and helpful, explaining in street language the protocols and policies of staying in the ICU: from visitation limitations to parental presence requirements.
I was impressed. Both of these women were competent, able to connect with a shy little girl of 3 years, and they provided answers to all of our questions - they have helped to significantly prepare us for our time next week at Childrens'.
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So, we're all set for Monday's surgery and a week at Childrens'. This weekend, we marry off Katie and Nate up at the Seminary, then church on Sunday, and then off we go. They tell us that there's wireless internet throughout most of the hospital, so there's a good chance I can continue updating the blog to keep you in the loop (depending on the level of sleep deprivation).
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